|
NM_001364171.2:c.467A>G
MANE Select
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NP_001351100.1:p.Glu156Gly
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ENST00000674294.1:c.467A>G
MANE Select
|
ENSP00000501363.1:p.Glu156Gly
|
|
NM_001364171.1:c.467A>G
|
NP_001351100.1:p.Glu156Gly
|
|
NM_144577.3:c.356A>G
|
NP_653178.3:p.Glu119Gly
|
|
NM_144577.4:c.356A>G
|
NP_653178.3:p.Glu119Gly
|
|
ENST00000315396.7:c.356A>G
|
ENSP00000318429.7:p.Glu119Gly
|
|
ENST00000474199.5:n.484A>G
|
|
|
ENST00000474199.6:c.467A>G
|
ENSP00000501357.1:p.Glu156Gly
|
|
ENST00000504608.6:n.325-344A>G
|
|
|
ENST00000674207.1:c.*175A>G
|
ENSP00000501374.1:n.*175A>G
|
|
XM_005259413.2:c.467A>G
|
XP_005259470.1:p.Glu156Gly
|
|
XM_005259414.2:c.467A>G
|
XP_005259471.1:p.Glu156Gly
|
|
XM_005259414.3:c.467A>G
|
XP_005259471.1:p.Glu156Gly
|
|
XM_005259415.2:c.467A>G
|
XP_005259472.1:p.Glu156Gly
|
|
XM_005259415.3:c.467A>G
|
XP_005259472.1:p.Glu156Gly
|
|
XM_011527515.1:c.356A>G
|
XP_011525817.1:p.Glu119Gly
|
|
XM_011527515.2:c.356A>G
|
XP_011525817.1:p.Glu119Gly
|
|
XM_011527516.1:c.356A>G
|
XP_011525818.1:p.Glu119Gly
|
|
XM_011527516.2:c.356A>G
|
XP_011525818.1:p.Glu119Gly
|
|
XM_011527517.1:c.467A>G
|
XP_011525819.1:p.Glu156Gly
|
|
XM_011527518.1:c.467A>G
|
XP_011525820.1:p.Glu156Gly
|
|
XM_017027483.1:c.191A>G
|
XP_016882972.1:p.Glu64Gly
|
|
XM_024451782.1:c.506A>G
|
XP_024307550.1:p.Glu169Gly
|
|
XM_024451783.1:c.467A>G
|
XP_024307551.1:p.Glu156Gly
|